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  2. Acephate - Wikipedia

    en.wikipedia.org/wiki/Acephate

    Acephate is an organophosphate foliar and soil insecticide of moderate persistence with residual systemic activity of about 10–15 days at the recommended use rate. It is used primarily for control of aphids, including resistant species, in vegetables (e.g. potatoes, carrots, greenhouse tomatoes, and lettuce) and in horticulture (e.g. on roses and greenhouse ornamentals).

  3. Imidacloprid - Wikipedia

    en.wikipedia.org/wiki/Imidacloprid

    Imidacloprid is a systemic insecticide belonging to a class of chemicals called the neonicotinoids which act on the central nervous system of insects. The chemical works by interfering with the transmission of stimuli in the insect nervous system. Specifically, it causes a blockage of the nicotinergic neuronal pathway.

  4. Terbufos - Wikipedia

    en.wikipedia.org/wiki/Terbufos

    Terbufos is a chemical compound used in insecticides and nematicides. It is part of the chemical family of organophosphates. It is a clear, colourless to pale yellow or reddish-brown liquid and sold commercially as granulate. [5]

  5. List of insecticides - Wikipedia

    en.wikipedia.org/wiki/List_of_insecticides

    This is a list of insecticides. These are chemical compounds which have been registered as insecticides. Biological insecticides are not included.

  6. Sulfoxaflor - Wikipedia

    en.wikipedia.org/wiki/Sulfoxaflor

    Sulfoxaflor is a systemic insecticide, acts as a neurotoxin to affected insects, and kills through contact or ingestion.. Sulfoxaflor is classified for use against sap-feeding insects as a sulfoximine, which is a sub-group of insecticides that act as nicotinic acetylcholine receptor (nAChR) competitive modulators.

  7. Spirotetramat - Wikipedia

    en.wikipedia.org/wiki/Spirotetramat

    It is a systemic insecticide that penetrates plant leaves when sprayed on. It is ambimobile , being transported both upwards and downwards through vascular bundles . [ 5 ] In plants, it is hydrolyzed to the enol form by cleavage of the central ethoxycarbonyl group .